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NCT07511920Not yet recruiting

A Multicenter Cohort Study of Duchenne and Becker Muscular Dystrophy in Western Chinese Children

A Real-World, Multicenter Cohort Study on the Natural History of Duchenne and Becker Muscular Dystrophy in Children From Western China

Source: ClinicalTrials.gov · Last updated 6 Apr 2026

Brief summary (registry, in English)

This is a prospective, multicenter, longitudinal observational cohort study aimed at understanding the progression of Duchenne Muscular Dystrophy (DMD). The primary objective is to identify and integrate key biomarkers from multiple sources-including motor function assessments, body composition (muscle and fat distribution), clinical laboratory tests, and cardiopulmonary imaging-to delineate comprehensive disease trajectories. By analyzing how these factors change over time in a large cohort, the study seeks to develop a robust model that can identify patterns of disease progression. The ultimate goal is to generate evidence that may aid in forecasting individual patient outcomes and inform the future development of personalized rehabilitation and therapeutic strategies.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
500 (estimated)
First submitted
30 Mar 2026
Start date
20 Apr 2026
Primary completion date
30 Dec 2028
Lead sponsor
West China Second University Hospital
NCT number
NCT07511920

What you commit to

  • Study type: Observational
  • Planned participants: 500
  • From 20 Apr 2026 to the primary completion date, 30 Dec 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Participants with other neuromuscular disorders that may confound natural history data
  • Participation in another interventional clinical trial that could affect disease progression

Other

  • Severe comorbidities that prevent completion of study assessments
  • Inability to provide informed consent or comply with study procedures

Who the study is looking for

  • Male participants with genetically confirmed diagnosis of Duchenne Muscular Dystrophy (DMD) or Becker Muscular Dystrophy (BMD)
  • Age range: 1 to 18 years old (adjust to your actual age limit)
  • Ability to complete study assessments and follow-up visits
  • Participants or legal guardians provide written informed consent

Age in the registry: 1 year to 18 years · Sex: Male

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
West China Second University Hospital, Sichuan University
Coordinator of this site? Confirm its status
ChengduChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.